A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737213



Internal ID160879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:116987036..116999589hg38UCSC Ensembl
chrX:116121004..116133557hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3812554
hg1912554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432478
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737213
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00104058


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